ClinVar Miner

Submissions for variant NM_002880.4(RAF1):c.1807C>T (p.Leu603=)

dbSNP: rs1420280008
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002214851 SCV002368726 likely benign RASopathy 2021-08-05 criteria provided, single submitter clinical testing

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